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Onur Selim Kilic

Publications and source records attributed to Onur Selim Kilic.

2 recordsLinked to original sources

Cylindrical Geodesic Flow Matching for Quasiperiodic Physiological Signal Transformation

Paired translation between quasiperiodic physiological waveforms (i.e., recovering a target oscillatory signal from the source) is central to the interpretation of cardiovascular signals derived from wearables placed at different body locations. This source-to-target mapping in these problems carries inherent geometric structure: the phase wraps around the cycle and must be treated as a circular variable, the amplitude remains strictly positive, and the beat-to-beat alignment can drift unpredictably across cycles and subjects. While deep neural networks have been used for phase estimation and complex-valued signal modeling, prior work does not explicitly learn phase transport between paired signals. Consequently, neither endpoint-supervised regression nor the standard affine path used in flow matching accounts for this phase--amplitude structure. We introduce \emph{cylindrical geodesic flow matching} for paired cardiovascular waveform translation. We show that the standard affine path used in flow matching distorts intermediate amplitude and instantaneous frequency when interpolating between quasiperiodic signals; replacing it with a closed-form geodesic on the phase--amplitude cylinder eliminates these artifacts and converts each training pair into dense, geometry-consistent velocity supervision. On zero-shot photoplethysmography and limited-support seismocardiography adaptation benchmarks, our method consistently outperforms interpolation baselines and matches or exceeds direct supervised prediction, reducing Hilbert Transform, $L_2$, and Dynamic Time Warping distance by up to ${\sim}15\%$ over the strongest competing baseline. These results suggest that bridge geometry is a critical inductive bias for flow matching on oscillatory signal translation.

cs.AI↗

Guideline2Graph: Profile-Aware Multimodal Parsing for Executable Clinical Decision Graphs

Clinical practice guidelines are long, multimodal documents whose branching recommendations are difficult to convert into executable clinical decision support (CDS), and one-shot parsing often breaks cross-page continuity. Recent LLM/VLM extractors are mostly local or text-centric, under-specifying section interfaces and failing to consolidate cross-page control flow across full documents into one coherent decision graph. We present a decomposition-first pipeline that converts full-guideline evidence into an executable clinical decision graph through topology-aware chunking, interface-constrained chunk graph generation, and provenance-preserving global aggregation. Rather than relying on single-pass generation, the pipeline uses explicit entry/terminal interfaces and semantic deduplication to preserve cross-page continuity while keeping the induced control flow auditable and structurally consistent. We evaluate on an adjudicated prostate-guideline benchmark with matched inputs and the same underlying VLM backbone across compared methods. On the complete merged graph, our approach improves edge and triplet precision/recall from $19.6\%/16.1\%$ in existing models to $69.0\%/87.5\%$, while node recall rises from $78.1\%$ to $93.8\%$. These results support decomposition-first, auditable guideline-to-CDS conversion on this benchmark, while current evidence remains limited to one adjudicated prostate guideline and motivates broader multi-guideline validation.

cs.CV↗